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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Rebiject II — 3 UDI-DI variants, MDR (Ares Trading SA)

MD Atlas
Ares Trading SA

Data from EUDAMED, last updated May 23, 2026

Rebiject II

4054839Rebiject2DD

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Ares Trading SA

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Device characteristics

Active deviceAdministers medicine

Identity & classification

Basic UDI-DI: 4054839Rebiject2DD
Device name: Rebiject II
Device model: Rebiject II
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 10, 2022

Manufacturer & authorised representative

Manufacturer

Name: Ares Trading SA
SRN: CH-MF-000021799
Country: Switzerland
Email: ATSA_PRRC@merckgroup.com
Phone: +41 58 432 32 00

Authorised representative

Name: Merck Healthcare KGaA
SRN: DE-AR-000007181
Country: Germany

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GEH41K2AJMHNJQDM4D69WE0H

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Rebiject II04065266543391
Rebiject II04065266543407
Rebiject II04065266543384